Rvot wire capturing (rwc) system in mitral valve cerclage annuloplasty

ABSTRACT

A mitral cerclage annuloplasty apparatus comprising of a catheter with a blocking member and a capturing member. The blocking member is in the shape of a pigtail or a balloon, and is configured on the distal portion of the catheter preventing the catheter from traversing through an unsafe zone thereby enabling the catheter to pass through the safe zone. This prevents damage to critical cardiac tissues. The capturing member is adapted for puffing out a RVOT cerclage wire into the IVC, and comprises of an expandable and collapsible mesh so that the RVOT cerclage wire is captured and directed into the IVC through the safe zone. Thus the RVOT cerclage wire is passed through the RV without damaging the heart tissue forming a complete circle around the mitral valvular annulus.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims the benefit of U.S. ProvisionalApplication No. 61/871,353 filed on Aug. 29, 2013; Korean PatentApplication No. 10-2014-0052674 filed on Apr. 30, 2014; and KoreanPatent Application No. 10-2014-0092817 filed on Jul. 22, 2014, which areincorporated herein by reference in its entirety.

FIELD OF INVENTION

The present invention generally relates to techniques and devices forcardiovascular valve repair, particularly annuloplasty techniques anddevices in which tensioning elements are positioned to treatregurgitation of the mitral valve in which mitral valve cerclage wire iscaptured and passed through the “safe zone” within the heart withoutdamaging critical cardiac structures.

BACKGROUND

The heart is at the center of human circulatory system that pumps bloodthrough our body unidirectionally. In order for the heart to effectivelykeep this unidirectional flow of blood, it must have properlyfunctioning valves that prevent back flow through its system, orregurgitation. The heart is divided into four chambers, right and leftatria, and right and left ventricles. The mitral valve (MV) separatesthe left atrium from the left ventricle while the tricuspid valve (TV)separates the right atrium (RA) from the right ventricle (RV).

Generally, valves should open and close completely with every heartbeator contraction. Incomplete opening and closing of the valves causeimproper flow of blood. Valvular diseases are divided into twocategories, regurgitation and stenosis. Regurgitation is a failure ofvalve to close completely and stenosis is a failure of valve to opencompletely.

Mitral regurgitation (MR) is a common cardiac valve disorder whereleakage of blood flow occurs due to an incomplete closure of the MV.Over time, MR burdens the heart and worsens its ability to pump bloodproperly eventually leading to a heart failure.

Traditional treatment of a worsening MR requires an open heart surgerywith thoracotomy, cardiac arrest and cardiopulmonary bypass. Once thechest is open and access to the heart is gained, the MV is eitherrepaired or replaced using an artificial or porcine valve.

Although very effective, this open-heart procedure is a high-risksurgery accompanied by substantial morbidity, mortality and prolongedrecovery. The mortality due to the surgery itself can be as high as 5%.Hence, the procedure is reserved only for those with severe symptomaticMR and often not offered to patients who are too weak or vulnerable orhave significant co-morbidity.

This high morbidity and mortality rates of an open-heart surgery havemotivated further research to develop safer and less risky alternatives.Much of the research involves percutaneous approaches with the use ofcardiac catheterization. Recently, this inventor filed a PCTInternational Application number PCT/US2007/023836 and PCT Internationalpublication number WO2008/060553 on a percutaneous approach to repairinga MR, “The MV cerclage coronary sinus annuloplasty (MVA),” which areincorporated herein in its entirety.

Briefly explained, a catheter is placed at the coronary sinus afteraccessing the RV through the jugular vein, and then a cerclage wire ispassed through the proximal septal vein and then through the rightventricular outflow tract (“RVOT”). Then the cerclage wire is pulledinto the RV thus placing the cerclage wire circumferentially around themitral annulus. Once the cerclage wire is positioned, tension is appliedtightening the MV and bringing together the two leaflets of the MV.

Further, in the published U.S. Patent Application Nos. 2005/0216039 and2010/0049314, tensioning material is introduced around the MV annulususing a secondary catheter, such as a steerable guide wire orcanalization catheter. The MV annulus is accessed by a number ofdifferent percutaneous approaches, including access from and through thecoronary sinus. Cerclage wire is placed around the mitral annulus thentension is applied re-opposing the leaflets of the MV and reducing thedefect.

While percutaneous cerclage annuloplasty is promising in valve repair,the procedure is technically demanding especially in proper positioningof the tension material around the valvular annulus to provide theproper plane of cerclage. Particularly, as the tensioning materialtraverses through the heart in its intramyocardial trajectory, there isa significant risk of tissue entrapment that limits the procedure andcan result in serious adverse outcomes.

For example, in mitral cerclage annuloplasty, as the cerclage wireleaves the coronary sinus and enters the RVOT of the RV, if the cerclagewire must be grabbed and pulled through the RV then through the superiorvena cava (SVC) or inferior vena cava (IVC). As the suture materialenters the RVOT, if it is not grabbed right away and pulled into the RV,then it can undermine the ventricular structures such as chordaetendonae of the tricuspid valve (TV), the papillary muscles, themoderator band and other valvular trabeculae resulting in tissueentrapment.

If tissue entrapment is not averted, entrapped tissues can be transectedand irreversibly damaged resulting not only in failure of the procedurebut also in other serious complications.

For this purpose, a special space between RV and RA can be defined asthe “safe zone.” The safe zone is defined as an imaginary space in whichthe cerclage wire can safely deliver therapeutic tension withoutdamaging the TV or the moderator band. It should be an enclosed circularspace bordered by (1) the TV leaflet and its subvalvular structures suchas the chordae of TV and the papillary muscle, and (2) the moderatorband. The remaining spaces between the RV and the RA other than the“safe zone” is defined here as the “unsafe zone.” Therefore, a needexists for a procedure and a device that facilitates proper positioningof the cerclage wire while preventing entrapment of the ventriculartissues.

SUMMARY OF THE DISCLOSURE

The present invention includes methods, apparatus and devices for valverepair for minimally invasive, percutaneous cerclage annuloplasty. Inparticular, methods, apparatus and devices of the present inventionfacilitate MV cerclage annuloplasty. Specifically, as the cerclage wiretraverses through the RV via the RVOT exit, methods and devices of thepresent invention are provided for properly guiding and capturing thecerclage wire through the “safe zone” averting entrapment of thecritical cardiac structures.

For this purpose, a special space between RV and RA can be defined asthe “safe zone.” The safe zone is defined as an imaginary space in whichthe cerclage wire can safely deliver therapeutic tension withoutdamaging the TV or the moderator band of the RV. It should be anenclosed circular space bordered by (1) the TV leaflet and itssubvalvular structures such as the chordae of TV and the papillarymuscle, and (2) the moderator band. The remaining spaces between the RVand the RA other than the “safe zone” is defined here as the “unsafezone.”

In an exemplary embodiment, there is featured a method for performing aMV cerclage annuloplasty by introducing a cerclage capture device intothe vasculature of a patient, traversing the capture device through thesafe zone, methods of testing or ensuring that the capturing devicetraversed through the safe zone, positioning the capturing device at anideal location of a cerclage trajectory, capturing the cerclage wire,and guiding the cerclage wire back through the safe zone preventingcapture, entrapment or damage to critical cardiac structures.

In accordance with the present invention, the ideal cerclage trajectorycomprises the coronary sinus, the basal interventricular septum, theRVOT exit, the RV and the IVC. An exemplary embodiment comprises acatheter with a blocking member and a capturing member. The blockingmember is configured on the distal portion of the catheter. The blockingmember prevents the catheter from traversing through an unsafe zone andenables the catheter to pass through a safe zone thereby circumventingdamage to the tricuspid valvular structures and the moderator band ofthe right ventricle. The capturing member is configured proximal to theblocking member, wherein the capturing member is adapted for pulling outa RVOT wire through the IVC. The RVOT wire is positioned in the RVthrough the SVC and the CS prior to being captured by the capturingmember. The blocking member is generally configured in the shape of apigtail or in the shape of a balloon that is inflatable and deflatableusing a control located outside of the patient's body. The capturingmember further comprises a mesh which is collapsible and expandableusing a control located outside of the patient's body. When the mesh isexpanded, the RVOT wire passes through the mesh, and when the mesh iscollapsed, the RVOT wire is securely grabbed by the mesh enabling thecatheter to pull out the RVOT wire into the IVC. In another embodiment,the capturing member further comprises a magnet adapted for magneticallycapturing the RVOT wire.

Further, the catheter comprises of a lumen adapted for passing a guidewire through the catheter. The surface of the capturing member can alsobe formed of a radio-opaque material adapted for visualizing thecapturing catheter to confirm its location radiographically. Yet, inanother embodiment, the capturing member comprises of a central lumencatheter, an outer catheter and a mesh. The central lumen catheter holdsthe guide wire, wherein the outer catheter holds the central lumencatheter enabling the central lumen catheter to move in and out. Thedistal portion of the mesh is gathered and secured to the central lumencatheter and the proximal portion of the mesh is gathered and secured tothe outer catheter. Additionally, the capturing member comprises of atleast one connector(s) which attaches the mesh to the central lumencatheter allowing the connector(s) to move back and forth causing themesh to expand and collapse thereby forming a D-shape when the mesh isexpanded.

In another exemplary embodiment of the present invention, there isanother method for directing a RVOT wire into the IVC in cerclageannuloplasty. This method comprises of inserting a safe-zone catheterthrough the IVC, passing through a safe zone of the RV, preventingpassage through an unsafe zone thereby circumventing damage to thetricuspid valvular structures and the moderator band of the RV, andpositioning the distal end of the safe-zone catheter at the RV and thePulmonary Artery (PA), while positioning the RVOT wire in the RV throughthe SVC and the CS. Then a guide wired is inserted through a lumen ofthe safe-zone catheter, the safe-zone catheter is removed while keepingthe guide wire in its place, a capturing catheter is inserted along theguide wire to the RV to capture the RVOT wire, and the RVOT wire isdirected so that the capturing catheter steers the captured RVOT wireinto the IVC.

The safe zone is further defined as an imaginary space in which thecerclage material can safely traverse through the right ventricle anddeliver therapeutic tension without damaging the TV and the moderatorband of the RV, wherein the safe zone is an enclosed circular spacebordered by (1) the subvalvular structures such as the TV leaflet,chordae of TV, and the papillary muscle, and (2) the moderator band, andwherein the remaining space between the RV and the RA other than thesafe zone is defined here as the unsafe zone.

In this exemplary body, a blocking member is further comprised on thedistal portion of the safe-zone catheter, wherein the blocking memberprevents the safe-zone catheter from traversing through the unsafe zoneand enables the safe-zone catheter to pass through the safe zone therebycircumventing damage to the tricuspid valvular structures and themoderator band of the RV. The blocking member is generally configured inthe shape of a pigtail, or in the shape of a balloon that is inflatableand deflatable using a control located outside of the patient's body.The capturing catheter further comprises a mesh which is collapsible andexpandable also using a control located outside of the patient's body.When the mesh is expanded, the RVOT wire passes through the mesh, andwhen the mesh is collapsed, the RVOT wire is firmly grabbed by the meshenabling the capturing catheter to pull out the RVOT wire through theIVC. The capturing catheter further comprises a magnet adapted formagnetically capturing the RVOT wire. Each of the safe-zone catheter andthe capturing catheter further comprises a lumen adapted for passing aguide wire through.

Furthermore, the outer surface of the capturing catheter is formed of aradio-opaque material adapted for visualizing the capturing catheter toconfirm its location radiographically. The capturing catheter furthercomprises a central lumen catheter, an outer catheter and a mesh whereinthe central lumen catheter which holds a wire. The outer catheter holdsthe central lumen catheter enabling the central lumen catheter to moveback and forth within the outer catheter. The distal portion of the meshis gathered and secured to the central lumen catheter, and the proximalportion of the mesh is gathered and secured to the outer catheter. Thecapturing catheter further comprises at least one connector(s) whichattaches the mesh to the central lumen catheter allowing theconnector(s) to move back and forth along the central lumen cathetercausing the mesh to expand and collapse thereby forming a D-shape whenthe mesh is expanded.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows anatomical structures and the safe trajectory for the MVcerclage annuloplasty wire exiting the RVOT into the RV and then exitingthrough the IVC. Also shown are the potentially vulnerable cardiacstructures that can be entrapped and damaged.

FIG. 2 shows a close up anatomical view of a wire passing through thesafe zone and a wire passing through the unsafe zone.

FIG. 3 shows another close up anatomical view of the wires in the safezone and the unsafe zone.

FIG. 4 is a schematic drawing of the MV cerclage annuloplasty RWCcatheter device comprising the wire, the wire catheter, the mesh and themesh catheter.

FIGS. 5 and 6 show a schematic view of the RWC catheter device inoperation. First, the RWC catheter device is traversed through the safezone and placed in the PA near the RVOT exit. Second, the mesh isexpanded. Third, the RVOT cerclage wire entering the RV through the RVOTexit passes through the mesh. Fourth, the mesh is collapsed capturingthe RVOT cerclage wire. Finally, the RWC wire capturing catheter isdirected into IVC bringing the captured RVOT cerclage wire with itthrough the safe zone.

FIG. 7 is another embodiment of MV cerclage annuloplasty RWC devicecomprising a safe-zone catheter having a balloon-shaped blocking member.Balloon is inflated to prevent the catheter from passing through theunsafe zone. Due to the size of the inflated balloon, the catheter canonly pass through the safe zone.

FIG. 8 is a drawing of another embodiment of MV cerclage annuloplastyRWC device comprising a safe-zone catheter having a pigtail-shapedblocking member on the distal end of the catheter and having a meshproximal to the pigtail-shaped blocking member.

FIG. 9 a shows a wall stent currently used as a self expanding stent inan angioplasty procedure requiring modifications to be used as the meshin the RWC catheter device.

FIG. 9 b is a schematic drawing of the self expanding mesh with closedupper part and a sheath or a catheter covering the mesh. The mesh sheathor the catheter can be used to control the expansion size of the mesh.

FIG. 10 is an anatomical view of the RVOT cerclage wire traversingthrough the SVC and the CS. Then the RVOT cerclage wire exits the CSthrough the RVOT into the RV.

FIG. 11 shows a drawing of the MV cerclage annuloplasty RWC devicecomprising a safe-zone catheter having a pigtail-shaped blocking memberon the distal end of the catheter, and a guide wire passing through thelumen of the catheter.

FIG. 12 shows a drawing of another embodiment of the MV cerclageannuloplasty RWC device comprising a capturing catheter with a mesh onthe distal end of the catheter.

FIG. 13 shows a drawing of another embodiment of MV cerclageannuloplasty RWC device comprising a safe-zone catheter having aballoon-shaped blocking member on the distal end of the catheter, and amesh proximal to the balloon-shaped blocking member.

FIG. 14 shows a drawing of another embodiment of MV cerclageannuloplasty RWC device comprising a capturing catheter with a D-shapedmesh wherein FIG. 14(a) shows the D-shaped mesh in its collapsed state,and FIG. 14(b) shows the D-shaped mesh in its expanded state.

FIG. 15 shows a drawing of the capturing catheter with the D-shaped meshin a heart, wherein FIG. 15(a) shows the D-shaped mesh in its collapsedstate, and FIG. 15(b) shows the D-shaped mesh in its expanded state.

DETAILED DESCRIPTION

The present invention feature methods and devices for repairing acardiac valve in a patient. In particular, methods and devices are fortreatment of valvular regurgitation in a cerclage annuloplastyprocedure. It is noted, while the methods and devices described inparticular is in connection with the MV regurgitation repair, suchmethods and devices can also be utilized for repairs of other valves.The detailed disclosure of the RVOT Wire Capturing (RWC) system methodsand devices will be disclosed.

Methods of the current invention generally include ensuring the RVOTwire, which has entered the RV through the SVC, the CS and the RVOT,safely passes through the safe zone into the IVC without damaging the TVstructures and the moderator band.

Methods of the invention generally include the RWC catheter devicecomprising a safe-zone catheter, a guide wire that passes through thecatheter lumen, and a RVOT wire capturing catheter will be discussed indetail. Additionally, an embodiment where the safe-zone catheter and theRVOT wire capturing catheter functioning as unibody will be discussed indetail as well.

In MV cerclage annuloplasty procedure, a wire is inserted into a tubethat has passed through the SVC and the CS. Then a catheter is insertedover the wire through the SVC and the CS. At that point, a contrastmedia is injected into the catheter to visualize and confirm thelocation of catheter within the CS. Then the wire is removed and theRVOT wire is introduced through the catheter. Subsequently, the RVOTwire passes through the basal interventricular septum exiting throughthe RVOT into the RV, and thus, the RVOT wire is named as the RVOTcerclage wire. In another words, in MV cerclage annuloplasty, the RVOTcerclage wire is defined as a cerclage wire that passes through theideal trajectory of the coronary sinus, the interventricular septum andthe RVOT into the RV thus encircling the MV.

In FIG. 10 is a schematic drawing of the heart showing the RVOT cerclagewire 104 as it traverses through the SVC 101, the CS and the RVOT 105into the RV.

In MV cerclage annuloplasty procedure, a RVOT cerclage wire 104traverses through the SVC 101, the CS and the RV then back through theSVC 101 thus forming a circle around the MV.

In order to steer the RVOT cerclage wire back into the SVC, the currentinvention comprises devices and methods to direct the RVOT cerclage wire104 first into the IVC 102.

In order to direct the RVOT cerclage wire into the IVC, first, thesafe-zone catheter is inserted through the IVC into the RV passingthrough the safe zone. Then a guide wire is passed through the safe-zonecatheter, thus ideally positioning at the PA. Then, the safe-zonecatheter is removed and the RVOT cerclage wire capturing catheter isinserted over the guide wire into the RV positioning at the PA. ThenRVOT cerclage wire is captured by the capturing catheter and thecatheter is directed to the IVC steering the captured RVOT cerclage wireinto the IVC. Then a snare is introduced through the SVC which can grabthe RVOT cerclage wire from the IVC into the SVC, thus completing thecircle around the MV.

The current invention includes devices and methods for traversingthrough the safe zone of the RV in a MV cerclage annuloplasty procedurecomprising a safe-zone catheter, a guide wire that passes through theIVC into the RV, a RVOT cerclage wire capturing catheter, and methodsfor using the said devices for directing the ROVT wire into the IVC.

The capturing catheter refers to the catheter used to capture the RVOTcerclage wire and since the capturing catheter directs the RVOT cerclagewire into the IVC, the catheter may be called RVOT cerclage wiresteering device.

In accordance with the current MV cerclage annuloplasty invention, priorto capturing the RVOT cerclage wire, a guide wire enters into the RV andends at the PA via the safe-zone catheter which traverses through thefemoral vein, the IVC, the RV and the PA. Here, the guide wire is namedsince the purpose of the guide wire is to guide the capturing catheterinto the RV. Thus the guide wire 103 must traverse through the safe zoneof the RV.

FIG. 1 shows an anatomical structures and the safe trajectory for the MVcerclage annuloplasty wire exiting the RVOT into the RV and the unsafetrajectory where the potentially vulnerable cardiac structures that canbe entrapped and damaged. FIG. 2 and FIG. 3 show an anatomical view of awire passing through the safe zone 120 and a wire passing through theunsafe zone.

FIGS. 1-3 show the critical cardiac structures in the RV such as the TVleaflets, the chordae of TV 150, papillary muscles 160 and the moderatorband 170. These valvular structures and the moderator band are criticalto the proper functioning of the RV, therefore, such structures shouldnot be damaged by cerclage wire or catheters. Accordingly, in MVcerclage annuloplasty procedure the safe-zone catheter should traversethrough the safe zone wherein the safe zone is an enclosed circularspace bordered by (1) the subvalvular structures such as the TV leaflet,chordae of TV, and the papillary muscle 160, and (2) the moderator band170. The remaining space between the RV and the RA other than the safezone is defined here as the unsafe zone. Hence the unsafe zone is thespace in the RV where the subvalvular structures such as the TV leaflet,chordae of TV and the papillary muscle, and the moderator band can bedamaged by the cerclage wire.

FIG. 2 clearly shows the difference of the safe zone 220 and the unsafezone. As shown in FIG. 2 and FIG. 3 , if the catheter passes through theunsafe zone and tension is applied in this pathway, critical hearttissues can be seriously and irreversibly damaged. Therefore, a cerclagewire or a catheter must pass through the safe zone 220 and whether acerclage wire or a catheter passed through the safe zone must beconfirmed.

Thus, safe-zone catheter refers to a catheter that passes through thesafe zone and can be confirmed that it indeed has traversed through thesafe zone.

In the current invention, the safe-zone catheter comprises aballoon-shaped blocking member or pigtail-shaped blocking member.Additionally, the safe-zone catheter is inserted through the IVC insteadof the SVC then is directed through the RV and into PA.

FIGS. 7, 8 and 11 disclose methods for verifying whether or not thecatheter or the cerclage wire passed through the safe zone, and methodsfor preventing the passage of the catheter or the cerclage wire throughthe unsafe zone.

FIG. 7 shows one embodiment of the safe-zone catheter of the currentinvention with a balloon-shaped blocking member, and the FIG. 8 showsanother embodiment of the safe-zone catheter with a pigtail-shapedblocking member 810 and a mesh 830 located proximal to thepigtail-shaped blocking member. FIG. 11 shows the safe-zone catheterwith the pigtail-shaped blocking member 113 and a guide wire 111 passingthrough the lumen of the safe-zone catheter.

First, according to the FIG. 7 , a balloon-shaped blocking member is onthe distal end of the safe-zone catheter preventing the passage of thesafe-zone catheter through the unsafe zone.

The blocking member of the safe-zone catheter provides a method offreely passing through the safe zone of the TV and the RV whilepreventing the passage through the unsafe zone. Namely, the blockingmember prevents the safe-zone catheter from passing through the unsafezone and assists the blocking member to traverse only through the safezone.

The safe-zone catheter with the balloon-shaped blocking member firstenters through the IVC, then air is injected into the balloon using theoutside control thus assisting the safe-zone catheter to traverse onlythrough the safe zone. In other words, once the balloon enters into theunsafe zone, further advancement into the heart is prevented. Hence,when the inflated balloon no longer advances, the safe-zone catheter canbe repeatedly withdrawn and re-entered until the catheter enters throughthe safe zone freely. Also, the reason why the safe-zone catheter issemi-rigid and the PA is approached from the IVC is to prevent thecatheter from entering into a portion of the unsafe zone between themoderator band and the RV wall.

FIG. 8 shows the pigtail-shaped blocking member positioned at the distalend of the safe-zone catheter. Upper left picture 800 in FIG. 8 showsthe pigtail-shaped blocking member positioned at the distal end of thesafe-zone catheter, and central picture in FIG. 8 shows thepigtail-shaped blocking member 810 positioned at the distal end 820 ofthe safe-zone catheter and a mesh situated proximal to thepigtail-shaped blocking member. In other words, the central picture inFIG. 8 shows the combined safe-zone catheter 820 and the cerclage wiredcapturing catheter 830.

As shown in FIG. 8 , since the catheter has a pigtail-shaped distal end810, the catheter is able to pass through the safe zone of the RV to thePA. The enlarged size of the pigtail-shaped end acts as the blockingagent thereby assisting the safe passage of the safe-zone catheter. Ifpig-tail shaped safe-zone catheter enters into the unsafe zone, it canno longer advance through the heart. When the safe-zone catheter doesnot advance, it can be withdrawn and re-advanced repeatedly until itadvances further through the safe zone into the PA.

Meanwhile, FIG. 11 shows a drawing of the MV cerclage annuloplasty RWCdevice comprising a safe-zone catheter having a pigtail-shaped blockingmember 113 on the distal end of the catheter 112, and a guide wire 111passing through the lumen of the safe-zone catheter. The distal end 113of the safe-zone catheter is shaped in a pigtail-shape so that thesafe-zone catheter can pass through the safe zone, and the safe-zonecatheter comprises a lumen that allows the passage of a guide wire 111.Also, the reason why the safe-zone catheter is semi-rigid and the PA isapproached from the IVC is to prevent the catheter from entering into aportion of the unsafe zone between the moderator band and the RV wall.

In an experiment using a 40-50 kg pig, this inventor selectively used apigtail and a balloon that was 1 cm in diameter to pass through the safezone. The inventor verified that Pigtail or balloon greater than 1 cm indiameter was not able to pass into the unsafe zone. Therefore, in orderto pass through the safe zone, the pigtail or the balloon needs begreater than 1 cm in diameter approximately.

Once safe-zone catheter passes through the safe zone and is positionedin the PA, a guide wire is inserted through the safe-zone catheter.Preferable, the guide wire should be passed into the PA and positionedat the entry of the PA. Then the safe-zone catheter is removed keepingthe guide wire positioned at the PA. Then the capture catheter isthreaded over the guide wire through the safe zone into the PA tocapture the RVOT cerclage wire.

FIG. 4 is a schematic drawing of the capture catheter of the MV cerclageannuloplasty comprising the wire 400, the wire catheter 410, the mesh420 and the mesh catheter 430. In other words, the RVOT cerclage wirewhich passed through the SVC or the IVC then through theinterventricular septum exiting through RVOT into the RV is captured bythe capture catheter 520 and directed from the PA into the IVC. Thecapture catheter 520 is named to indicate that it functions to capturethe RVOT cerclage wire 540, and thus can also be called RVOT wirecapture catheter.

FIG. 4 also shows the mesh of the capture catheter device. The mesh 510remains collapsed until the capture catheter reaches the RV and isexpanded once it is the RV near the PA to facilitate easy passage of theRVOT cerclage wire 540 through the mesh 420. Once the RVOT cerclage wirepasses through the mesh, the mesh is collapsed capturing the RVOTcerclage. In other words, the mesh is collapsed or expanded from acontrol located outside the patient's body and when it is expanded, themesh is configured so that the RVOT cerclage wire easily passes throughthe mesh, and when it is collapsed, it can firmly grab the RVOT cerclagewire.

To summarize the capture catheter, the mesh is passed through the IVCinto the RV near the PA. Since the capture catheter passes over theguide wire which has already traversed through the safe zone, thecapture catheter and the mesh placed on the distal portion of thecapture catheter can only pass through the safe zone of the RV.Radiographic imaging can be utilized to confirm the position of the meshand the RVOT cerclage wire. The mesh composes of radio-opaque marker sothat it is adapted for visualizing to confirm its locationradiographically. Then the mesh is expanded to allow easy passage of theRVOT cerclage wire. Once the RVOT cerclage wire passes through the mesh,the mesh is collapsed using the control located outside the patient'sbody capturing the RVOT cerclage wire.

FIGS. 5 and 6 show how the capture catheter captures the RVOT cerclagewire. FIG. 5(a) shows the capture catheter 520 positioned inside the RV,FIG. 5(b) shows the capture catheter with the expanded mesh, FIG. 5(c)and FIG. 6(d) show the RVOT cerclage wire 630 passing through theexpanded mesh 610, FIG. 6(e) shows collapsed mesh with captured RVOTcerclage wire, and FIG. 6(f) shows the capture catheter being directedinto the IVC thus steering with it the captured RVOT cerclage wire.

Though it is not shown in the Figures, instead of the mesh, the capturemember of the capture catheter can be formed of a magnetic material tocapture the RVOT cerclage wire magnetically. The RVOT cerclage wire orthe distal end of the RVOT cerclage wire must be also formed of amagnetic material.

FIG. 9(a) shows a wall stent 900 currently used as a self expandingstent in an angioplasty procedure requiring modifications to be used asthe mesh in the RWC catheter device. FIG. 9(b) is a schematic drawing ofthe self expanding mesh with closed upper part 910 and a sheath or acatheter covering the mesh. The mesh sheath or the catheter can be usedto control the expansion size of the mesh.

FIG. 12 shows a drawing of another embodiment of the MV cerclageannuloplasty RWC device comprising a capturing catheter 121 with a mesh124 positioned on the distal end 123 of the capture catheter. Since thecapture catheter is inserted over the guide wire into the RV, thecapture catheter has a lumen to allow the passage of the guide wire. Theproximal or the distal portion of the mesh can be formed of radio-opaquemarker 123 so that it can be visualized radiographically from theoutside to confirm the location of the mesh and the capture catheter.

Although, the safe-zone catheter and the capture catheter are describedabove separately, the two catheters can be combined into one unit 131 sothat it has can have both functions and is included within the scope ofthis invention. This is shown and briefly described in FIG. 8 and alsoin FIG. 13 .

FIG. 13 shows a drawing of another embodiment of MV cerclageannuloplasty RWC device comprising a safe-zone catheter 131 having aballoon-shaped blocking member 136 on the distal end of the catheter,and a mesh 135 proximal to the balloon-shaped blocking member 136. FIG.8 and FIG. 13 both contain the safe-zone catheter's blocking member 136,810 as well as the capture catheter's capturing member in one body.

RVOT cerclage wire is captured by the capturing catheter and thecatheter is directed to the IVC steering the captured RVOT cerclage wireinto the IVC. Then a snare is introduced through the SVC to grab theRVOT cerclage wire from the IVC into the SVC, thus completing the circlearound the MV annulus.

As describe above, during the MV cerclage annuloplasty procedure, themethod for steering the RVOT cerclage wire into the IVC comprises ofpositioning the RVOT cerclage wire in the RV through either the SVC, theCS and the inter ventricular septum, and positioning the safe-zonecatheter at the PA through the IVC and the safe zone of the RV. Then aguide wire can be inserted through the safe-zone catheter whichtraverses through the safe zone. Once the guide wire is positioned atthe PA, the safe-zone catheter is removed and the capture catheter isadvanced over the guide wire through the safe zone to the PA. Once thecapture catheter is positioned in the PA, the RVOT wire can be capturedand steered out towards the IVC by directing the capture catheter outtoward the IVC.

If the safe-zone catheter and the capture catheter is combined into onedevice, the method for steering the RVOT cerclage wire into the IVCcomprises of first, positioning the RVOT cerclage wire at the RV afterit passes through the SVC, the CS and the inter ventricular septum.Meanwhile the combined MV cerclage annuloplasty catheter is positionedat the PA after traversing through the IVC and the safe zone of the RV.Then, using the capture member of the combined MV cerclage annuloplastycatheter, the RVOT cerclage wire is captured and steered out towards theIVC by directing the combined MV cerclage annuloplasty catheter with thecapture member out toward the IVC.

Once the RVOT cerclage wire is steered into the IVC, then a snare isintroduced through the SVC to grab the RVOT cerclage wire from the IVCinto the SVC, thus completing the circle around the MV annulus.

FIG. 14 shows a drawing of another embodiment of MV cerclageannuloplasty RWC device comprising a capturing catheter with a D-shapedmesh 143,147 and FIG. 15 shows a drawing of the capturing catheter withthe D-shaped mesh 155 in a heart.

FIG. 14(a) and FIG. 15(a) both show the D-shaped mesh 143, 153 in itscollapsed state, and FIG. 14(b) and the FIG. 15(b) both show theD-shaped mesh 147,156 in its expanded state. FIG. 15(a) shows the mesh153 before it has completely entered the RV.

Referring to FIG. 14 and FIG. 15 , the capturing catheter of the MVcerclage annuloplasty RWC device comprises of the outer catheter 144,146, 155, 158, the central lumen catheter 142, 156, 154 and the D-shapedmesh 143, 147, 153, 156. The distal portion of the D-shaped mesh isgathered and fixed to the central lumen catheter 142, 156, 154 and theproximal portion of the D-shaped mesh 143, 147, 153, 156 is gathered andfixed to the outer catheter 144, 146, 155, 158.

The central lumen catheter 142, 156, 154 has an open internal lumenwhich holds a guide wire so that the capture catheter can be insertedover the guide wire to the RV.

The central lumen catheter is placed inside lumen of the outer catheterso that it can move back and forth within the lumen of the outercatheter.

The capture catheter is inserted over the guide wire passing through thesafe zone into the RV. When the outer catheter is pushing inwardly fromthe outside of the body, then the outer catheter will move inwardly anddistally over the central lumen catheter thus expanding the mesh.

Preferably, when the mesh is expanded, it forms the shape of the capitalletter “D” conforming to the shape of the RV so that the RVOT cerclagewire which has entered the RV through the interventricular septum canmore easily pass through the expanded mesh. Further, when the mesh isthe shape of a capital letter “D,” thus it is able to expand the mostdue to the anatomical shape of the RV such that the RVOT cerclage wirewill naturally fall through the expanded mesh enabling precision in theability to steer the RVOT wire into the IVC.

Referring to the FIG. 14 , in the current invention, in order for themesh 143,147 to be in D-shape when it is expanded, the capturingcatheter comprises at least one connector(s) 145 which attaches but doesnot fix the mesh to the central lumen catheter 142 allowing theconnector(s) 145 to move freely back and forth along the central lumencatheter 142, 147 so that the mesh 143, 147 can expand and collapseforming a D-shape when the mesh is expanded 147. Since the connector(s)145 is always attached to one side of the central lumen catheter 142,when the mesh expands, it can fully expand towards the opposite,unattached side of the RV in the shape of letter “D.”

Although not illustrated in the Figures, within one outer catheter, thesafe-zone catheter and the capture catheter can be inserted. Asdiscussed previously, the combined MV cerclage annuloplasty catheterwith the safe-zone catheter and the capture catheter comprises ofblocking member positioned proximal to the distal end of the catheterand the capture member positioned on proximal to the blocking member.Alternatively, a separate safe-zone catheter and a separate capturecatheter can be positioned inside one single outer catheter.

Having illustrated and described the principles of the invention byseveral embodiments, it should be apparent that those embodiments can bemodified in arrangement and detail without departing from the principlesof the invention. Thus the invention includes all such embodiments andvariations thereof, and their equivalents.

1. A capture catheter comprising: a catheter having a distal end; and anexpandable capturing means mounted on the catheter, wherein thecapturing means consists of an expandable open mesh.
 2. The catheter ofclaim 1, wherein the mesh is radio-opaque or comprises a radio-opaquemarker.
 3. The catheter of claim 1, wherein the shape of the open meshconsists of a D-shape.
 4. The catheter of claim 1, wherein one side ofthe mesh has a greater radius of curvature than the other when the meshis in an expanded configuration.
 5. The catheter of claim 1, whereinthere is no covering over the open mesh.
 6. The catheter of claim 1,wherein there is no element covering over the open mesh.
 7. The catheterof claim 1, further comprising a control configured for expanding andcollapsing the mesh.
 8. The catheter of claim 1, further comprising aninflatable balloon mounted on the catheter at a location distal to theexpandable capturing means, wherein the inflatable balloon has aninflated diameter of one centimeter or greater.
 9. The catheter of claim1, wherein the catheter has a lumen.